List of bibliographic references
Number of relevant bibliographic references: 7.
List of associated KwdEn.i
Nombre de
documents | Descripteur |
|---|
| 2 | Female |
| 2 | Humans |
| 2 | Male |
| 1 | Alleles |
| 1 | Animals |
| 1 | Cell Line |
| 1 | Child, Preschool |
| 1 | Choanal Atresia (genetics) |
| 1 | Chromosomal Proteins, Non-Histone (genetics) |
| 1 | Death, Sudden, Cardiac (etiology) |
| 1 | Death, Sudden, Cardiac (pathology) |
| 1 | Diphosphates |
| 1 | Dominant character |
| 1 | Epigenesis, Genetic (genetics) |
| 1 | Exome (genetics) |
| 1 | Exon |
| 1 | Gene Deletion |
| 1 | Genes, Essential (genetics) |
| 1 | Genetic Complementation Test |
| 1 | Genetic Predisposition to Disease (genetics) |
| 1 | Genetics |
| 1 | Heterozygote |
| 1 | Infant |
| 1 | Inorganic Pyrophosphatase (genetics) |
| 1 | Inorganic Pyrophosphatase (metabolism) |
| 1 | Membrane Potential, Mitochondrial (genetics) |
| 1 | Mice |
| 1 | Mice, Inbred C57BL |
| 1 | Microbial Viability |
| 1 | Microphthalmos (genetics) |
| 1 | Mitochondria (enzymology) |
| 1 | Mitochondria (metabolism) |
| 1 | Mitochondria (pathology) |
| 1 | Mitochondrial Proteins (genetics) |
| 1 | Mitochondrial Proteins (metabolism) |
| 1 | Muscular Dystrophy, Facioscapulohumeral (genetics) |
| 1 | Mutation |
| 1 | Mutation (genetics) |
| 1 | Mutation, Missense |
| 1 | Mutation, Missense (genetics) |
| 1 | Nose (abnormalities) |
| 1 | Pierre Robin syndrome |
| 1 | Proton Pumps (deficiency) |
| 1 | Proton Pumps (genetics) |
| 1 | Proton Pumps (metabolism) |
| 1 | Saccharomyces cerevisiae (cytology) |
| 1 | Saccharomyces cerevisiae (enzymology) |
| 1 | Saccharomyces cerevisiae (genetics) |
| 1 | Saccharomyces cerevisiae Proteins (genetics) |
| 1 | Saccharomyces cerevisiae Proteins (metabolism) |
| 1 | Xenopus laevis (genetics) |
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|wiki= Wicri/Asie
|area= AustralieFrV1
|flux= UK
|étape= Analysis
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